Improvement Effect of Transcranial Direct Current Stimulation (tDCS) Applied During Exercise Training in Stroke Patients With Upper Limb and Hand Motor Function
- Conditions
- Stroke
- Interventions
- Device: tDCS stimulation with hand taskDevice: sham tDCS stimulation with hand task
- Registration Number
- NCT05275114
- Lead Sponsor
- Yun-Hee Kim
- Brief Summary
The purpose of this study was to improve the effect of Transcranial Direct Current Stimulation (tDCS) applied during exercise training in stroke patients with upper limb and hand motor function.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 24
- Patients aged 19 to 80 years
- Less than 58 FMA Upper scores
- Patients whose lesions do not include stimulation regions
- Patients with stroke with more than 3 months of onset
- Difficult to communicate due to severe language impairment.
- Accompanied by an existing serious neurogenic disease
- Existing significant psychiatric disorders such as major schizophrenia, bipolar disorder
- If there are difficulties in conducting the research
- Any patients who are judged by the investigator to be difficult to participate in this study
- Patients with contraindicated MRI scans
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Hand Tasks + M1(1mA) & aIPS(1mA) tDCS tDCS stimulation with hand task 20 minutes of Hand Taks + applying 30 minutes of M1(1mA) \& aIPS(1mA) tDCS and fNIRS Hand Tasks + Sham tDCS sham tDCS stimulation with hand task 20 minutes of Hand Tasks + 30 minutes of sham tDCS and fNIRS
- Primary Outcome Measures
Name Time Method Change in Fugl-Meyer Assessment Session 0 (initial visit);; Session 10 (at approximatel 4 weeks) The score is a stroke-specific, performance-based impairment index. The degree of impairment of upper and lower limbs is measured.
- Secondary Outcome Measures
Name Time Method Change in Box and Block test Baseline(initial visit); Session 10 (at approximatel 4 weeks) The test is used to measure the gross manual dexterity of a patient, or of a person using an upper limb prosthetic device.
Change in Grip & Tip pinch strength Baseline(initial visit); Session 10 (at approximatel 4 weeks) The test is to measure the maximum isometric strength of hand, forearm, and finger muscles.
Changes in Brain activation of resting-state functional MRI [Time Frame: session 0 (initial visit); session 10 (at approximately 4 weeks)] Measure of Neuroplasticity
Change in 9-hole pegboard test Baseline(initial visit); Session 10 (at approximatel 4 weeks) The test is a standardized, quantitative assessment used to measure finger dexterity of a patient.
Change in Sequential finger tapping reaction time and accruacy Baseline(initial visit); Session 10 (at approximatel 4 weeks) Response time and accuracy are measured during finger tapping task.
Change in Jebsen-Taylor hand function test Baseline(initial visit); Session 10 (at approximatel 4 weeks) This test is a standardized and objective measure of fine and gross motor hand function using simulated activities of daily living (ADL).
Changes in motor evoked potential [Time Frame: session 0 (initial visit); session 10 (at approximately 4 weeks)] Resting motor threshold (rMT) and amplitude of motor evoked potential in first dorsal interosseous muscle are measured. These outcomes are measured by transcranial magnetic stimulation over the motor hotspot. The rMT is defined as the minimum stimulus intensity that produced a minimal motor evoked response at rest. The amplitude means peak to peak of the muscle response.
Trial Locations
- Locations (1)
Samsung Medical Center
🇰🇷Seoul, Korea, Republic of